Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives

Detalhes bibliográficos
Autor(a) principal: Vale,Juliana A.
Data de Publicação: 2012
Outros Autores: Faustino,Wagner M., Zampieri,Davila de S., Moran,Paulo J. S., Rodrigues,José A. R., de Sá,Gilberto F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000800005
Resumo: In this work we report the use of lanthanide nitrates [Ln(NO3)3] acting as catalyst in direct one-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazoles derivatives from ketones, nitriles and nitric acid. This is the first example of one-pot synthesis of benzoyl- and acetyl 1,2,4-oxadiazoles derivatives preparation using acetophenones derivates with electron-donator groups.
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spelling Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivativeslanthanide nitratesLewis acids1,2,4-oxadiazole derivatesIn this work we report the use of lanthanide nitrates [Ln(NO3)3] acting as catalyst in direct one-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazoles derivatives from ketones, nitriles and nitric acid. This is the first example of one-pot synthesis of benzoyl- and acetyl 1,2,4-oxadiazoles derivatives preparation using acetophenones derivates with electron-donator groups.Sociedade Brasileira de Química2012-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000800005Journal of the Brazilian Chemical Society v.23 n.8 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000002info:eu-repo/semantics/openAccessVale,Juliana A.Faustino,Wagner M.Zampieri,Davila de S.Moran,Paulo J. S.Rodrigues,José A. R.de Sá,Gilberto F.eng2012-09-14T00:00:00Zoai:scielo:S0103-50532012000800005Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-09-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
title Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
spellingShingle Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
Vale,Juliana A.
lanthanide nitrates
Lewis acids
1,2,4-oxadiazole derivates
title_short Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
title_full Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
title_fullStr Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
title_full_unstemmed Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
title_sort Lanthanide nitrates as Lewis acids in the one-pot synthesis of 1,2,4-oxadiazole derivatives
author Vale,Juliana A.
author_facet Vale,Juliana A.
Faustino,Wagner M.
Zampieri,Davila de S.
Moran,Paulo J. S.
Rodrigues,José A. R.
de Sá,Gilberto F.
author_role author
author2 Faustino,Wagner M.
Zampieri,Davila de S.
Moran,Paulo J. S.
Rodrigues,José A. R.
de Sá,Gilberto F.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Vale,Juliana A.
Faustino,Wagner M.
Zampieri,Davila de S.
Moran,Paulo J. S.
Rodrigues,José A. R.
de Sá,Gilberto F.
dc.subject.por.fl_str_mv lanthanide nitrates
Lewis acids
1,2,4-oxadiazole derivates
topic lanthanide nitrates
Lewis acids
1,2,4-oxadiazole derivates
description In this work we report the use of lanthanide nitrates [Ln(NO3)3] acting as catalyst in direct one-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazoles derivatives from ketones, nitriles and nitric acid. This is the first example of one-pot synthesis of benzoyl- and acetyl 1,2,4-oxadiazoles derivatives preparation using acetophenones derivates with electron-donator groups.
publishDate 2012
dc.date.none.fl_str_mv 2012-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000800005
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000800005
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012005000002
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.23 n.8 2012
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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